Metochondria Respiratory Diseases Diseases: Symptoms, Causes and Treatment

Mitochondrial chain defective by mitochondria is a cell member that transmits electrons to oxygen and produces energy, as these processes are performed by a protein system within the mitochondria, called the mitukandria. The presence of an imbalance of birth in one of the respiratory series protein leads to reducing the work of the chain, which is why a lack of energy and the accumulation of toxic oxygen derivatives. The majority of mitochondria -respiratory proteins are coded by core genome, which is the sum of genes in the organism (nuclear genomic), and only a small number of them are coded by Metacandry genome, so in addition to regular physical genetics, it is also possible to transmit the disease with judgment. In each cell in the body there are thousands of copies of the Mtdna DNA DNA, where this mutation usually harms only part of it and thus produces two groups, and this situation is called the various blood plasma (heteroplasmia). The different level of blood plasma at each of the children varies, and consequently it is likely that the same mother causes a different sharpness of disease, such as in divided tissues, such as: blood cells and intestinal cells in which the different blood plasma level will change during life and thus the symptoms fall. Symptoms of mitochondria breathing diseases include the most important symptoms of the following: high level of lactic acid with body fluids. Changes in the level of alanine protein. Ketones change a presumption of metocandry disease in the blood apron. Heart thickness and failure of his work. Disability. Spasm. Visual nerve degeneration. Liver insufficiency. Kidney disease. Myopathy. All of this is only a small portion of the possible symptoms, as not all these symptoms occur in all patients, and the course of the disease can progress, corrected or withdraw. Causes and factors of the risk of diseases of the mitochondria breathing chain in most people. The primary mitochondria disease is a genetic condition that can inherit any transmission from parents to their children in different ways. In normal circumstances, the child inherits the genes in the pairs of one none of the mother and the other of the father, but the child with Mitochondria does not receive a natural pair of genes from parents. The gene mutated, which means it has become flawed, that is, it has changed. The most important methods of genetics that cause the disease include the following: 1. The recessive chromosome heroes. 2. The prevailing physical chromosome inheritance. This child receives one copy of the gene from any parents, and there is a 50% possibility that every child in the family inherits mitochondria. 3.. The inheritance of mitochondria in this unique kind of genetics The mitochondria contains its DNA, where only the mitochondria deviations caused by mutation of mitochonders caused only from mothers. If this is the way in which inherited mitochondria is, there is a 100% chance that every child in the family inherits mitochondria. 4. Random mutations sometimes develop genes that are not inherited from one of the parents. Complications of the diseases of the breathing chain mitochondria, as the muscles and neurons have especially high energy needs, especially muscle and neurological problems are common features of mitochondria, and the most important complications include: poor eyesight. Error. Diabetes. Growth stops. A person with mitochondria usually suffers from two or more of these cases, some of which happen together regularly, so that it is compiled in syndromes. Diagnosis of mitochondria -breathing disease The diagnosis depends on enzymatic examinations of the efficacy of the respiratory chain in the blood cells through cellular transplantation of the skin cells, in the muscle or in every other participating tissue, it is not possible to measure the effectiveness of the effectiveness of the protein. The prenatal diagnosis can be determined in a portion of mitochondria disease in which enzymatic deficiency appears on the skin cells, or if the gear -infected gene is known, it is also possible to distinguish people who carry the mutation when the mutation is known. The treatment of the diseases of the mitochondria breathing chain does not achieve the treatment of diseases of the mitochondria breathing chain that exist these days, and it is acceptable to give antioxidants, or substances that enable energy balance or different breathing vehicles, reducing the substances of the lactate in the blood. There are no treatments for mitochondria diseases, but the treatment can help reduce symptoms or health weakening. Treatment ranges from patient to patient and depends on the specified mitochondria disease that has been diagnosed and strengthened. However, there is no way to predict the patient’s response to treatment or prediction of how the disease affects this person in the long run, as two people will not respond in the same way in the same way, even if they have the same illness. Metochondria treatments may include the following: 1. Vitamins and nutritional supplements, including the assistant -enzyme Q10; Complex vitamins, especially thiamine, riboflavin and alpha lipoic acid. 2. Doing exercises, including endurance and resistance exercises, as it is done to increase muscle size and power, and include endurance, hiking, running, swimming, dancing, cycling and others. Resistance and strength exercises include weight -up exercises, arms reinforcement exercises, knee extension, weight lifting and others. 3.. The maintenance of energy because you do not make much effort to do in a short time. 4. Other treatments may include speech therapy, physical therapy, respiratory therapy and career therapy. Prevention of mitochondria -breathing diseases avoids situations that can aggravate your medical condition, and that includes: Exposure to cold or heat. Famous and malnutrition. Lack of sleep. Difficult situations. Use of alcohol. Smoke. The consumption of single sodium glutamate.